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FDA 510(k), K102366, FINESS ENDOSCOPE
FDA 510(k), K102366, FINESS ENDOSCOPE
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510(K) Number: K102366
Device Name: FINESS ENDOSCOPE
Manufacturer: Entellus Medical, Inc.
Device Classification Name: nasopharyngoscope (flexible or rigid)
Regulation Number: 874.4760
Classification Product Code: EOB
Date Received: 08/20/2010
Decision Date: 02/15/2011
Regulation Medical Specialty: Ear Nose & Throat
Device Name: FINESS ENDOSCOPE
Manufacturer: Entellus Medical, Inc.
Device Classification Name: nasopharyngoscope (flexible or rigid)
Regulation Number: 874.4760
Classification Product Code: EOB
Date Received: 08/20/2010
Decision Date: 02/15/2011
Regulation Medical Specialty: Ear Nose & Throat
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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